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MAC 5000 ECG ANALYSIS SYSTEM

K014108 Class II Special
Decision Date
2002-01-10
Sponsor / Applicant
General Electric Medical Systems Information Techn

Technical Specification

510(k) Submission ID K014108
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2002-01-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MAC 5000 ECG ANALYSIS SYSTEM received FDA 510(k) clearance under submission number K014108, sponsored by General Electric Medical Systems Information Techn. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2002-01-10.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.